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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,063
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,821–1,840 of 19,905 recalls

FDA Recall United States Terminated Historical recordClass II

Monkey Spit

Product
Monkey Spit "Atomic Mop" BBQ Sauce, 12 fl oz (355ml) glass b…
Reason
Barbeque sauce product contains undeclared allergen listing of (Milk) in product ingredient listing from sub-ingredient Butter.
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Monkey Spit

Product
Monkey Spit "Swamp Mop" BBQ Sauce, 12 fl oz (355ml) glass bo…
Reason
Barbeque sauce product contains undeclared allergens (soy) contained in sub-ingredient
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Inflectra (infliximab-dyyb), For injection, 100mg per vial, packaged in 10 mL single-dose vial, Rx only, Mfd by: CELLTRION, INC, Dist. by: Pfizer Labs, Division of Pfizer Inc., New York, NY 10001, NDC 0069-0809-01

by McKesson

Reason
cGMP Deviations: Product intended for quarantine was inadvertently distributed.
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 20 mg, packaged in a) 30 Unit Doses (3x10 blister packs) NDC 0904-7043-04 and b) 100 Unit Doses (10x10 blister packs) NDC 0904-7043-61, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA.

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason
CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Prograf (tacrolimus) capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Product of Japan, Distributed by: Astellas Pharma US, Inc., Northbrook, IL 60062, NDC 0469-0607-73.

by Astellas Pharma US Inc.

Reason
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Astagraf XL (tacrolimus extended-release capsules) 0.5 mg, 30-count bottles, RX Only, Product of Japan, Distributed by: Astellas Pharma US Inc., Northbrook, IL 60062, NDC 0469-0647-73.

by Astellas Pharma US Inc.

Reason
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Company, Inc, 768 Route 10, Gilsum NH, 03448 UPC 6 34084 47150 2

by The W.S. Badger Company, Inc.

Reason
Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Iovate Health Sciences USA Inc.

Product
Alpha Test 120 count Black labeled plastic bottle, 12 bottle…
Reason
Presence of cathine in product
Published
February 5, 2025
Distribution
Domestic and foreign distribution:NC, CA…

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Vegetable Bowl 850065403380 13 oz (368g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Vegetable Bowl 860010507131 26 oz (738g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Vegetable Ranch Tray No Dip Small 850054894335 19.5 oz (553…
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Family Cobb Salad 850054894625 22 oz (623g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Individual Garden Salad 850054894618 12 oz (340g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Individual Greek Salad 850054894649 12 oz (340g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Family Garden Salad 850054894601 24 oz (679g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Individual Cobb Salad 850054894632 11 oz (311g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Southwest Salad 850065403069 Net Wt: 4oz (113g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Cucumber w/ Ranch Snack Cup 850065403144 Net Wt: 9.5oz (269g…
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Cucumber Slices W/Tajin 850053685699 10 oz (284g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC dba Yummi Sushi

Product
Cucumber Bowl with Ranch dip 850054894519 15oz (425g)
Reason
Potential Salmonella
Published
February 5, 2025
Distribution
CO

View recall →

Data last updated:

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.